| Total (93) | D2 (10) | D3 (32) | D4 (51) | |
|---|---|---|---|---|
| Premier | 2 (2.15 %) | 2 (3.92 %) | ||
| Deuxième | 5 (5.38 %) | 1 (10.00 %) | 2 (6.25 %) | 2 (3.92 %) |
| Troisième | 2 (2.15 %) | 2 (3.92 %) |
| Eq | Saison | Div | Tour | Match | Neg | Plc | IC | ADV |
|---|---|---|---|---|---|---|---|---|
| KIHa | 2010 | 3 | 6 | KIHa(68.0)-HYAb(68.0) | -259 | 16 | 1.0 | 8.0 |
| KIHa | 2010 | 3 | 1 | HYAb(61.5)-KIHa(74.5) | -214 | 12 | 5.0 | 5.0 |
| KIHb | 2009 | 4 | 10 | KIHb(31.0)-KAKc(44.0) | -306 | 2 | 11.0 | 1.0 |
| KIHb | 2009 | 4 | 8 | QUAa(56.0)-KIHb(21.0) | -219 | 8 | 5.0 | 6.0 |
| KIHa | 2009 | 4 | 7 | SABd(25.0)-KIHa(53.0) | -326 | 7 | 6.0 | 1.0 |
| KIHb | 2009 | 4 | 6 | PHEb(49.0)-KIHb(29.0) | -277 | 10 | 4.0 | 7.0 |
| KIHb | 2009 | 4 | 5 | KAKc(50.0)-KIHb(28.0) | -211 | 6 | 7.0 | 4.0 |
| KIHb | 2009 | 4 | 3 | KIHb(27.0)-QUAa(51.0) | -221 | 5 | 7.0 | 4.0 |
| KIHb | 2009 | 4 | 2 | KAKb(55.0)-KIHb(23.0) | -384 | 13 | 2.0 | 8.0 |
| KIHb | 2009 | 4 | 1 | KIHb(15.0)-PHEb(57.0) | -445 | 7 | 6.0 | 6.0 |
| KIHb | 2008 | 4 | 10 | PHEb(57.0)-KIHb(21.0) | -201 | 7 | 6.0 | 6.0 |
| KIHb | 2008 | 4 | 8 | YODc(33.0)-KIHb(45.0) | -207 | 6 | 7.0 | 2.0 |
| KIHb | 2008 | 4 | 7 | KIHb(32.0)-PHEb(46.0) | -102 | 1 | 12.0 | 0.0 |
| KIHb | 2008 | 4 | 5 | KIHb(44.0)-YODc(34.0) | -231 | 10 | 0.0 | 3.0 |
| KIHb | 2008 | 4 | 4 | SABd(43.0)-KIHb(35.0) | -234 | 5 | 8.0 | 3.0 |
| KIHb | 2008 | 4 | 3 | KIHb(41.0)-YODc(37.0) | -149 | 1 | 12.0 | 0.0 |
| KIHb | 2008 | 4 | 1 | KIHb(50.5)-SABd(27.5) | -261 | 14 | 0.0 | 6.0 |
| KIHb | 2007 | 4 | 10 | KIHb(23.0)-CINa(55.0) | -434 | 12 | 2.0 | 7.5 |
| KIHb | 2007 | 4 | 8 | ACJc(46.5)-KIHb(31.5) | -212 | 12 | 1.0 | 6.0 |
| KIHb | 2007 | 4 | 7 | KIHb(42.0)-PHEb(36.0) | -228 | 6 | 7.0 | 3.0 |
| KIHb | 2007 | 4 | 6 | KIHa(56.0)-KIHb(22.0) | -214 | 14 | 1.0 | 8.0 |
| KIHb | 2007 | 4 | 4 | KIHb(26.0)-NUPa(52.0) | -187 | 12 | 1.0 | 6.0 |
| KIHb | 2007 | 4 | 3 | KIHb(25.0)-ACJc(53.0) | -98 | 7 | 6.0 | 5.0 |
| KIHb | 2007 | 4 | 2 | PHEb(41.5)-KIHb(36.5) | -349 | 13 | 1.0 | 7.0 |
| KIHb | 2007 | 4 | 1 | KIHb(21.0)-KIHa(57.0) | -385 | 15 | 0.0 | 8.0 |
| KIHb | 2006 | 4 | 9 | KIHb(35.0)-ACJc(42.0) | -148 | 3 | 10.0 | 1.0 |
| KIHb | 2006 | 4 | 8 | KIHb(39.0)-CRSa(39.0) | -173 | 7 | 6.0 | 3.0 |
| KIHb | 2006 | 4 | 7 | BOUa(55.0)-KIHb(22.0) | -249 | 10 | 4.0 | 7.0 |
| KIHb | 2006 | 4 | 6 | KIHb(32.5)-CINa(45.5) | -267 | 4 | 9.0 | 3.0 |
| KIHb | 2006 | 4 | 5 | KIHb(35.0)-BOUb(43.0) | -254 | 7 | 6.0 | 3.0 |
| KIHb | 2006 | 4 | 4 | ACJc(39.0)-KIHb(38.0) | -134 | 6 | 7.0 | 3.0 |
| KIHb | 2006 | 4 | 2 | KIHb(21.0)-BOUa(57.0) | -274 | 11 | 3.0 | 7.0 |
| KIHa | 2005 | 3 | 10 | HELa(87.0)-KIHa(49.0) | -204 | 12 | 5.0 | 7.0 |
| KIHb | 2005 | 4 | 8 | FUNa(52.0)-KIHb(26.0) | -179 | 9 | 4.0 | 5.0 |
| KIHa | 2005 | 3 | 7 | PHEa(81.0)-KIHa(55.0) | -346 | 14 | 3.0 | 8.0 |
| KIHa | 2005 | 3 | 6 | KIHa(76.0)-MAKa(59.0) | -200 | 14 | 3.0 | 6.0 |
| KIHb | 2005 | 4 | 5 | KAKb(47.0)-KIHb(31.0) | -178 | 11 | 2.0 | 6.0 |
| KIHb | 2005 | 4 | 4 | KIHb(28.0)-PHEb(50.0) | -163 | 11 | 2.0 | 6.0 |
| KIHb | 2005 | 4 | 3 | KIHb(26.0)-FUNa(52.0) | -219 | 9 | 4.0 | 5.0 |
| KIHb | 2005 | 4 | 2 | CBFa(51.0)-KIHb(27.0) | -164 | 8 | 5.0 | 5.0 |
| KIHb | 2004 | 4 | 8 | KIHb(28.0)-KAKa(50.0) | -200 | 8 | 5.0 | 5.0 |
| KIHa | 2004 | 3 | 7 | KIHa(58.0)-ROYb(78.0) | -306 | 15 | 2.0 | 8.0 |
| KIHb | 2004 | 4 | 6 | KIHb(23.0)-PHEb(55.0) | -249 | 6 | 7.0 | 5.0 |
| KIHb | 2004 | 4 | 5 | ASSa(57.0)-KIHb(21.0) | -293 | 11 | 3.0 | 7.0 |
| KIHa | 2004 | 3 | 3 | REJa(74.0)-KIHa(62.0) | -192 | 16 | 1.0 | 8.0 |
| KIHa | 2004 | 3 | 2 | ROYb(72.0)-KIHa(64.0) | -305 | 11 | 6.0 | 5.0 |
| KIHb | 2004 | 4 | 1 | PHEb(57.0)-KIHb(21.0) | -251 | 9 | 5.0 | 7.0 |
| KIHb | 2003 | 4 | 9 | KIHb(21.0)-SASa(57.0) | -305 | 11 | 3.0 | 7.0 |
| KIHb | 2003 | 4 | 8 | KIHb(32.0)-PHEb(46.0) | -220 | 8 | 5.0 | 5.0 |
| KIHb | 2003 | 4 | 7 | HAWa(52.0)-KIHb(26.0) | -181 | 7 | 6.0 | 5.0 |
| KIHb | 2003 | 4 | 6 | KIHb(32.0)-ACJb(46.0) | -194 | 8 | 5.0 | 4.0 |
| KIHb | 2003 | 4 | 4 | SASa(49.0)-KIHb(29.0) | -367 | 8 | 5.0 | 5.0 |
| KIHb | 2003 | 4 | 3 | PHEb(55.0)-KIHb(23.0) | -277 | 12 | 2.0 | 7.0 |
| KIHb | 2003 | 4 | 2 | KIHb(24.0)-HAWa(54.0) | -213 | 7 | 6.0 | 5.0 |
| KIHb | 1983 | 3 | 9 | BORa(86.0)-KIHb(49.0) | -286 | 15 | 2.0 | 8.0 |
| KIHb | 1983 | 3 | 6 | GRIa(97.0)-KIHb(39.0) | -153 | 12 | 5.0 | 8.0 |
| KIHb | 1983 | 3 | 5 | KIHb(69.0)-BRAa(67.0) | -187 | 15 | 2.0 | 8.0 |
| KIHb | 1983 | 3 | 3 | KIHb(41.0)-ASSb(95.0) | -218 | 15 | 2.0 | 8.0 |
| KIHb | 1983 | 3 | 2 | RESa(55.5)-KIHb(79.5) | -122 | 4 | 12.5 | 1.5 |
| KIHb | 1983 | 3 | 1 | KIHb(54.0)-VALa(82.0) | -154 | 11 | 6.0 | 7.0 |
| KIHb | 1982 | 2 | 11 | MJAb(74.5)-KIHb(61.5) | -98 | 2 | 15.0 | 1.0 |
| KIHb | 1982 | 2 | 10 | KIHb(55.0)-MACa(80.0) | -219 | 9 | 8.0 | 5.0 |
| KIHb | 1982 | 2 | 8 | KIHb(67.0)-SACa(68.0) | -270 | 11 | 6.0 | 5.0 |
| KIHb | 1982 | 2 | 7 | LOUb(70.0)-KIHb(66.0) | -127 | 9 | 8.0 | 4.0 |
| KIHb | 1982 | 2 | 6 | KIHb(46.0)-SIRa(90.0) | -231 | 14 | 3.0 | 8.0 |
| KIHb | 1982 | 2 | 5 | SCBa(72.0)-KIHb(64.0) | -208 | 13 | 4.0 | 6.0 |
| KIHb | 1982 | 2 | 4 | WATb(86.0)-KIHb(50.0) | -209 | 13 | 4.0 | 8.0 |
| KIHb | 1982 | 2 | 3 | KIHb(55.0)-OUEb(81.0) | -254 | 16 | 1.0 | 8.0 |
| KIHb | 1982 | 2 | 2 | KIHb(48.0)-PICa(88.0) | -143 | 12 | 5.0 | 7.0 |
| KIHb | 1982 | 2 | 1 | PHEb(77.5)-KIHb(58.5) | -254 | 15 | 2.0 | 8.0 |
| HYAa | 1981 | 3 | 9 | ASSb(65.0)-HYAa(71.0) | -311 | 16 | 1.0 | 8.0 |
| HYAb | 1981 | 4 | 8 | YODa(78.5)-HYAb(57.5) | -88 | 5 | 12.0 | 3.0 |
| HYAb | 1981 | 4 | 7 | SRMa(48.0)-HYAb(88.0) | -122 | 3 | 14.0 | 0.0 |
| HYAa | 1981 | 3 | 6 | SABb(55.0)-HYAa(81.0) | -197 | 11 | 6.0 | 4.0 |
| HYAa | 1981 | 3 | 5 | HYAa(80.5)-SASa(55.5) | -96 | 9 | 7.5 | 2.5 |
| HYAb | 1981 | 4 | 4 | HYAb(67.0)-CINa(69.0) | -104 | 2 | 15.0 | 1.0 |
| HYAb | 1981 | 4 | 3 | PHEc(79.0)-HYAb(57.0) | -217 | 4 | 13.0 | 2.0 |
| HYAb | 1981 | 4 | 2 | HYAb(57.0)-BLOa(79.0) | -215 | 6 | 11.0 | 4.0 |
| HYAa | 1980 | 3 | 6 | RESa(65.0)-HYAa(71.0) | -376 | 15 | 2.0 | 7.0 |
| HYAa | 1980 | 3 | 5 | HYAa(65.0)-ASSb(71.0) | -277 | 16 | 1.0 | 8.0 |
| HYAa | 1980 | 3 | 4 | SABb(66.0)-HYAa(70.0) | -285 | 14 | 3.0 | 6.0 |
| HYAb | 1980 | 3 | 2 | ASSb(89.0)-HYAb(47.0) | -172 | 4 | 13.0 | 3.0 |
| HYAa | 1979 | 3 | 6 | HYAa(65.0)-SABb(71.0) | -126 | 2 | 15.0 | 0.0 |
| HYAa | 1979 | 3 | 5 | ASSb(72.0)-HYAa(64.0) | -370 | 15 | 2.0 | 7.0 |
| HYAa | 1979 | 3 | 4 | RESa(73.0)-HYAa(63.0) | -323 | 14 | 3.0 | 8.0 |
| HYAa | 1979 | 3 | 3 | SABb(88.0)-HYAa(48.0) | -249 | 14 | 3.0 | 8.0 |
| HYAa | 1979 | 3 | 2 | HYAa(68.0)-ASSb(68.0) | -226 | 2 | 15.0 | 0.0 |
| HYAa | 1979 | 3 | 1 | HYAa(75.0)-RESa(61.0) | -188 | 10 | 7.0 | 5.0 |
| HYAa | 1978 | 3 | 9 | CREa(50.0)-HYAa(86.0) | -321 | 8 | 9.0 | 3.0 |
| HYAa | 1978 | 3 | 7 | MJAb(80.0)-HYAa(56.0) | -224 | 9 | 8.0 | 6.0 |
| HYAa | 1978 | 3 | 5 | HYAa(80.0)-REBa(56.0) | -210 | 8 | 9.0 | 3.0 |
| HYAa | 1978 | 3 | 3 | ASSb(55.0)-HYAa(81.0) | -246 | 11 | 6.0 | 4.0 |
| HYAa | 1978 | 3 | 1 | HYAa(64.0)-MALc(72.0) | -101 | 4 | 13.0 | 2.0 |