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Putative copy number variants assessed by TaqMan assays.
| Gene symbol | CNV type | Variant carrier | Assay ID | Overlap CNV map1 | Proportion validated |
|---|---|---|---|---|---|
| SULT1A1 | Deletion | BRCA1 | 1 | Yes | 100% (8/8) |
| TERT | Deletion | BRCA2 | 1 | No | 0% (0/1) |
| 2 | No | 0% (0/1) | |||
| 3 | No | 33% (1/3) | |||
| LSP1 | Duplication | BRCA2 | 1 | No | 50% (1/2) |
CNV copy number variant. 1Zarrei et al (2015) stringent CNV map.
