Variant DetailsVariant: nsv428159Internal ID | 18277923 | Landmark | | Location Information | | Cytoband | 7p22.3 | Allele length | Assembly | Allele length | hg38 | 206370 | hg19 | 206370 | hg18 | 269217 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv450910, nssv450912, nssv450911, nssv450915, nssv450913, nssv450907, nssv450905 | Samples | HGDP01093, HGDP00476, HGDP00450, HGDP00467, NA19181, NA19257, HGDP00474 | Known Genes | FAM20C, LOC100507642 | 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) | nsv428159
| Frequency | Sample Size | 62 | Observed Gain | 7 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|