VALLBYVIKS JIP
Linebreeding statistics, 20 generations
- Inbreeding coefficient (full-depth value): 8.28%
- Unique ancestors in 20 generations (175 / 2097150) = 0.01%
- Total crosses walked (incl. repeats): 385
- The recorded pedigree runs out after 15 generations.
Min crosses: 2 · 78 repeated ancestors
| Name | Crosses | # | Lines | Blood % | Influence |
|---|---|---|---|---|---|
| GÖTTER-MAHLS SHANSHAN | 2D · 3S | 2 | 2 (1)(1) | 37.50% | 2x3 |
| TEXAS WAGONS DEAN LADY | 4d×2 · 5s×2 | 4 | 4 (2)(2) | 18.75% | 3x4 |
| GÖTTER-MAHLS SWEET-HEART | 3d · 4s | 2 | 2 (1)(1) | 18.75% | 3x4 |
| TAYLER OF GOTTER-MAHLS | 3D · 4S | 2 | 2 (1)(1) | 18.75% | 3x4 |
| CANDY OF BOYER | 5D×2 · 6S×3 · 6D · 7S · 7D | 8 | 8 (4)(4) | 14.06% | 4x4 |
| CASMY OF KAWASAKI SATSA | 5d×2 · 6s×2 | 4 | 4 (2)(2) | 9.38% | 4x5 |
| CATHARINE OF SHIRAKAWA NOGUCHI | 4S · 5D | 2 | 2 (1)(1) | 9.38% | 4x5 |
| GLORIA OF TAMANA | 4D · 5S | 2 | 2 (1)(1) | 9.38% | 4x5 |
| SECOND PEAT OF FUJIMILAND | 4D · 5S | 2 | 2 (1)(1) | 9.38% | 4x5 |
| ETHEL OF GROWING FIELD | 6d×2 · 7s×3 · 7d · 8s · 8d | 8 | 8 (4)(4) | 7.03% | 5x5 |
| FRESH BOYER OF UMIHIKOSOW | 6D×2 · 7S×3 · 7D · 8S · 8D | 8 | 8 (4)(4) | 7.03% | 5x5 |
| ANGEL PEET OF FUJIMILAND | 6D×2 · 7S×3 · 7D · 8S | 7 | 7 (4)(3) | 6.64% | 5x5 |
| SOPHIA OF MIURA | 7s · 7d×3 · 8s×5 · 8d · 9s · 9d | 12 | 12 (7)(5) | 5.86% | 5x6 |
| EDWARD BOYER OF GOLDEN STAR | 7S · 7D×2 · 8S×3 · 8D×2 · 9S · 9D | 10 | 10 (5)(5) | 4.69% | 5x6 |
| ANNA OF TSURUMI KISHIDA | 6d×2 · 7s×2 | 4 | 4 (2)(2) | 4.69% | 5x6 |
| ANN CATLAIR OF FUJIMILAND | 5d · 6s | 2 | 2 (1)(1) | 4.69% | 5x6 |
| BLUE ANTHONY OF FUJIMILAND | 5D · 6S | 2 | 2 (1)(1) | 4.69% | 5x6 |
| MY BELLE CROWN OF SHIRAKAWA NOGUCHI | 5S · 6D | 2 | 2 (1)(1) | 4.69% | 5x6 |
| SNOW MARQUISE OF SHIRAKAWA NOGUCHI (1975) | 5s · 6d | 2 | 2 (1)(1) | 4.69% | 5x6 |
| DIAMOND 11 VON HAUS FEUER LAND | 7S×3 · 8S · 8D×3 · 9D | 8 | 8 (4)(4) | 4.10% | 6x6 |
| FUJI OF MIURA | 7D×2 · 8S×4 · 8D · 9S · 9D | 9 | 9 (5)(4) | 3.91% | 6x6 |
| BLUES HANNA OF FUJIMILAND | 6s · 6d · 7s | 3 | 3 (2)(1) | 3.91% | 6x6 |
| BOSPHORUS OF BENNET KENNEL | 5S · 7S | 2 | 2 (2)(0) | 3.91% | 6x6 |
| BUNNY OF GROWING FIELD | 7d×2 · 8s×3 · 8d · 9s · 9d | 8 | 8 (4)(4) | 3.52% | 6x6 |
| HEIDY OF UMIHIKOSOW | 7d×2 · 8s×3 · 8d · 9s · 9d | 8 | 8 (4)(4) | 3.52% | 6x6 |
| MEL MURATA OF DIAMOND TOKYO | 7D×2 · 8S×3 · 8D · 9S · 9D | 8 | 8 (4)(4) | 3.52% | 6x6 |
| WHITE STAR OF SHIRAKAWA NOGUCHI | 6s · 7s · 7d · 8d | 4 | 4 (2)(2) | 3.52% | 6x6 |
| ALTARE OF TSURUMI KISHIDA | 6D · 7S · 7D | 3 | 3 (1)(2) | 3.13% | 6x6 |
| WHITE PRINCE OF LILAC KENNEL | 6S · 6D | 2 | 2 (1)(1) | 3.13% | 6x6 |
| CLARICE OF SNOW LIGHT | 8s · 8d×3 · 9s×5 · 9d · 10s · 10d | 12 | 12 (7)(5) | 2.93% | 6x7 |
| JUNIORS DANDY | 8S · 8D×3 · 9S×5 · 9D · 10S · 10D | 12 | 12 (7)(5) | 2.93% | 6x7 |
| VERDA OF SAINT PAUL | 8s · 8d×2 · 9s×3 · 9d×2 · 10s · 10d | 10 | 10 (5)(5) | 2.34% | 6x7 |
| ANGEL BABY OF FUJIMI LAND | 6s · 7d | 2 | 2 (1)(1) | 2.34% | 6x7 |
| DIAMOND 3 OF KUMAMOTO DOBASHISOW | 6S · 7D | 2 | 2 (1)(1) | 2.34% | 6x7 |
| DIAMOND III OF KUMAMOTO DOBASHISOW | 6S · 7D | 2 | 2 (1)(1) | 2.34% | 6x7 |
| STAR FUJI OF SHIRAKAWA NOGUCHI | 6s · 7d | 2 | 2 (1)(1) | 2.34% | 6x7 |
| SHIRO OF ARRINGTON KENNELS | 6s · 8s | 2 | 2 (2)(0) | 1.95% | 7x7 |
| SHIRO TETSU | 6S · 8S | 2 | 2 (2)(0) | 1.95% | 7x7 |
| WHITE LILY OF SHIRAKAWA NOGUCHI | 7s · 8s · 8d · 9d | 4 | 4 (2)(2) | 1.76% | 7x7 |
| PRO SAEGUSA | 7D · 8S · 8D | 3 | 3 (1)(2) | 1.56% | 7x7 |
| TAK OF TSURUMI KISHIDA | 7d · 8s · 8d | 3 | 3 (1)(2) | 1.56% | 7x7 |
| LILY (ROKU WA MANOR) | 9s · 9d×2 · 10s×3 · 10d×2 · 11s · 11d | 10 | 10 (5)(5) | 1.17% | < 7x7 |
| SHIRAOU (YASHIRO) | 9S · 9D×2 · 10S×3 · 10D×2 · 11S · 11D | 10 | 10 (5)(5) | 1.17% | < 7x7 |
| ANGEL PINA OF FUJIMILAND | 7s · 8d | 2 | 2 (1)(1) | 1.17% | < 7x7 |
| SHIRAGIKUHIME | 7s · 8d | 2 | 2 (1)(1) | 1.17% | < 7x7 |
| ANGEL OF GINSETSUSOW | 7s · 9s | 2 | 2 (2)(0) | 0.98% | < 7x7 |
| ATUKIE | 7S · 9S | 2 | 2 (2)(0) | 0.98% | < 7x7 |
| JUPITER OF SAZANAMISOW | 7S · 9S | 2 | 2 (2)(0) | 0.98% | < 7x7 |
| MARY | 7s · 9s | 2 | 2 (2)(0) | 0.98% | < 7x7 |
| KORRY | 8S · 10S | 2 | 2 (2)(0) | 0.49% | < 7x7 |
| PICHI OF SAZANAMISOW | 8s · 10s | 2 | 2 (2)(0) | 0.49% | < 7x7 |
| ROMIE | 8s · 10s | 2 | 2 (2)(0) | 0.49% | < 7x7 |
| RUBIAN OF KANEKO | 8S · 10S | 2 | 2 (2)(0) | 0.49% | < 7x7 |
| CHINNY OF ARAKAWA | 9S · 11S | 2 | 2 (2)(0) | 0.24% | < 7x7 |
| ELIZAR | 9s · 11s | 2 | 2 (2)(0) | 0.24% | < 7x7 |
| GON OF KAMOGAWA | 9S · 11S | 2 | 2 (2)(0) | 0.24% | < 7x7 |
| QUEEN | 9s · 11s | 2 | 2 (2)(0) | 0.24% | < 7x7 |
| CHERRY OF HEIANSOW | 10s · 12s | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| JOHNNY OF TAKEUCHI | 10S · 12S | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| KENNY | 10S · 12S | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| KING OF KINSEN | 10S · 12S | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| PIKOTE | 10s · 12s | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| RUBY OF HOPE TOKYO | 10S · 12S | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| SHIRO (F) | 10s · 12s | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| WHITE QUEEN OF ARAKAWA | 10s · 12s | 2 | 2 (2)(0) | 0.12% | < 7x7 |
| BOYA KOMORI | 11S · 13S | 2 | 2 (2)(0) | 0.06% | < 7x7 |
| FRICKER | 11s · 13s | 2 | 2 (2)(0) | 0.06% | < 7x7 |
| KENY ONO | 11S · 13S | 2 | 2 (2)(0) | 0.06% | < 7x7 |
| LILY OF ENDO | 11s · 13s | 2 | 2 (2)(0) | 0.06% | < 7x7 |
| MARY OF ARAKAWA | 11s · 13s | 2 | 2 (2)(0) | 0.06% | < 7x7 |
| ROCK OF ISHII | 11S · 13S | 2 | 2 (2)(0) | 0.06% | < 7x7 |
| CHERRY KOMORI | 12s · 13s · 14s · 15s | 4 | 4 (4)(0) | 0.05% | < 7x7 |
| CHERRY (KING OF KINSEN) | 12s · 14s | 2 | 2 (2)(0) | 0.03% | < 7x7 |
| ER | 12S · 14S | 2 | 2 (2)(0) | 0.03% | < 7x7 |
| LASU | 12S · 14S | 2 | 2 (2)(0) | 0.03% | < 7x7 |
| LURY | 12s · 14s | 2 | 2 (2)(0) | 0.03% | < 7x7 |
| SNOW OF GREENHILL | 12S · 14S | 2 | 2 (2)(0) | 0.03% | < 7x7 |
| TARO KOMORI | 13S · 15S | 2 | 2 (2)(0) | 0.02% | < 7x7 |
Crosses, Lines, Blood % and Influence are structural. Blood % (Percent of Blood / Genetic Contribution Coefficient) is Wright's ½^generation contribution summed over every cross, and Influence is its equivalent-cross restatement; rows are ranked by Blood % to surface top influencers. An asterisk marks an ancestor that also appears in the final (20th) generation, where the walk stops.