Table 1.
Information and genomic features of representative CNVb markers associated with known structural variations and predominant haplotypes
| Marker ID | Chromosome | Start position (Mb) | End position (Mb) | Associated genome feature | Associated gene | Number of lines |
|---|---|---|---|---|---|---|
| CNVb.67.1 | 1B | 0 | 239.3 | 1RS·1BL | Pm8/Sr31/Lr26/Yr9 | 111 |
| CNVb.67.2 | 1B | 0 | 236.7 | 1RS·7DL/7DS·1BL | Pm8/Sr31/Lr26/Yr9 | 16 |
| CNVb.162 | 1D | 412.1 | 412.5 | Glu-D1d (Dx5 + Dy10) haplotype | 430 | |
| CNVb.189 | 2A | 0 | 24.7 | 2NvS/2AS | Lr37/Yr17/Sr38 | 142 |
| CNVb.290 | 2B | 89.5 | 769.0 | Triticum timopheevii introgression | Sr36 | 2 |
| CNVb.540 | 3D | 592.0 | 616.0 | Thinopyrum ponticum introgression | 13 | |
| CNVb.647 | 4B | 30.5 | 31.1 | r-e-z deletion | Rht-B1/EamA-B/ZnF-B | 10 |
| CNVb.989 | 6B | 167.9 | 183.4 | perInv-6B | 33 |