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Sign inLine-breeding
6 shared ancestors
Closest: Temlee · 3×
Top earner in tree
Not recorded
Computed from the recorded parent links. 2 recorded birth years in this tree conflict — see the record warning in the tree.
A parent is recorded as born after its offspring. The tree keeps the recorded links and dates; they need checking before using this pedigree for breeding decisions.
Line-breeding detail — ancestors on both sides
Duplication and inbreeding across the 5 generations mapped for this dog. Deterministic lineage arithmetic — nothing here is a prediction.
Computed from the recorded parent links. 2 recorded birth years in this tree conflict — see the record warning in the tree.
Computed from the identified parent links recorded in this 5-generation window, including shared ancestors’ recorded inbreeding. Unknown founders are assumed unrelated; this is not a DNA measurement or certification of the source records. Displayed percentages are rounded. Every slot in this pedigree is recorded across this window; records that run deeper than 5 generations are still outside it.
Ancestors holding two or more positions in this pedigree, by share of this dog’s blood within the 5 mapped generations.
| Ancestor | Blood % | Generation 1 | Generation 2 | Generation 3 | Generation 4 | Generation 5 |
|---|---|---|---|---|---|---|
Waverly Supreme * |
| Date | Track | Dist | Box | Finish | Time | Grade | Wgt | 1st Sec | Mgn | Winner / 2nd | Race |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 23 Oct 04 | Cannington | — | — | — | 16.28s | GR 4 | — | — | — | — | — |
| 16 Oct 04 | Cannington | — | — | — | 12.18s | GR 3/4 | — | — | — | — | — |
| 25 Sept 04 | Cannington | — | — | — | 16.80s | GR | — | — | — | — | — |
| 18 Sept 04 | Cannington | — | — | — | 16.43s | OPEN | — | — | — | — | — |
| 11 Sept 04 | Cannington | — | — | — | 16.37s | GR 3/4 | — | — | — | — | — |
| 04 Sept 04 | Cannington | — | — | — | 16.36s | OPEN | — | — | — | — | — |
| 28 Aug 04 | Cannington | — | — | — | 16.41s | GR 4 | — | — | — | — | — |
| 22 Aug 04 | Cannington | — | — | — | 5.90s | GR 5 | — | — | — | — | — |
| 10 Aug 04 | Northam | — | — | — | 10.28s | OPEN | — | — | — | — | — |
| 03 Aug 04 | Northam | — | — | — | 10.42s | OPEN | — | — | — | — | — |
| 11 July 04 | Cannington | — | — | — | 5.98s | GR 3/4 | — | — | — | — | — |
| 03 July 04 | Cannington | — | — | — | 16.74s | GR 4 | — | — | — | — | — |
| 26 June 04 | Cannington | — | — | — | 12.14s | GR 4 | — | — | — | — | — |
| 13 June 04 | Cannington | — | — | — | 5.99s | GR 5 | — | — | — | — | — |
| 15 May 04 | Mandurah | — | — | — | 11.74s | GR 4 | — | — | — | — | — |
| 08 May 04 | Mandurah | — | — | — | 17.42s | GR 3/4 | — | — | — | — | — |
| 17 Apr 04 | Cannington | — | — | — | 12.03s | GR 3/4 | — | — | — | — | — |
| 08 Apr 04 | Cannington | — | — | — | 6.01s | GR 5 | — | — | — | — | — |
| 01 Apr 04 | Cannington | — | — | — | 6.06s | GR 5 | — | — | — | — | — |
| 25 Mar 04 | Cannington | — | — | — | 5.97s | GR 3/4 | — | — | — | — | — |
2 recorded positions. Share of the inbreeding coefficient: +1.56%.
| 18.8% |
| — |
| — |
| D1 |
| S1 |
| — |
Little Blade(1978)2 recorded positions. Share of the inbreeding coefficient: +0.78%. Sire side S 3.1%Dam side D 12.5% | 15.6% | — | — | D1 | — | S1 |
|---|
Temlee(1972)3 recorded positions. Share of the inbreeding coefficient: +0.78%. Sire side S 6.3%Dam side D 6.3% | 12.6% | — | — | — | D1 | S2 |
|---|
Octum(1967)2 recorded positions. No contribution to the inbreeding coefficient is recorded for this ancestor in this window. Sire side S 3.1%Dam side D 6.3% | 9.4% | — | — | — | D1 | S1 |
|---|
Supreme Fun(1969)2 recorded positions. No contribution to the inbreeding coefficient is recorded for this ancestor in this window. Sire side S 3.1%Dam side D 6.3% | 9.4% | — | — | — | D1 | S1 |
|---|
Benjamin John(1966)2 recorded positions. Share of the inbreeding coefficient: +0.20%. Sire side S 3.1%Dam side D 3.1% | 6.2% | — | — | — | — | S1D1 |
|---|
Counts show recorded positions, not percentages. G1 = parents. A dash means no occurrence in the recorded slots; unknown ancestry remains unknown. Tap an ancestor for its coefficient contribution.
