Table 1 Candidate intervals obtained through homozygosity mapping of three affected siblings and five unaffected individuals (three siblings and two parents). We detected six different candidate regions shared by the cases and not by the controls. The large CFA12 interval contains the putative causative variant. All coordinates are reported on the Canfam4 reference.
From: GTPBP2 in-frame deletion in canine model with non-syndromic progressive retinal atrophy
Chromosome | Start (bp) | End (bp) |
|---|---|---|
chr8 | 66,887,716 | 67,511,362 |
chr9 | 30,403,072 | 34,619,830 |
chr12 | 156,577 | 41,610,477 |
chr17 | 40,733,820 | 41,772,912 |
chr22 | 13,932,775 | 32,405,762 |
chr35 | 22,579,827 | 23,917,512 |
