Variant DetailsVariant: nssv453242Internal ID | 18273526 | Landmark | | Location Information | | Cytoband | 1q44 | Allele length | Assembly | Allele length | hg38 | 377316 | hg19 | 377315 | hg18 | 377315 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv428357 | Supporting Variants | | Samples | HGDP00471 | Known Genes | OR14C36, OR14I1, OR2G6, OR2T1, OR2T10, OR2T11, OR2T2, OR2T27, OR2T29, OR2T3, OR2T34, OR2T35, OR2T4, OR2T5, OR2T6 | Method | BAC aCGH | Analysis | Copy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006). | Platform | Sanger H. sapiens Whole Genome Tile Path 28.7k v3 | Comments | | Reference | Perry_et_al_2008b | Pubmed ID | 18775914 | Accession Number(s) | nssv453242
| Frequency | Sample Size | 62 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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