Variant DetailsVariant: nsv428290Internal ID | 18278054 | Landmark | | Location Information | | Cytoband | 1q31.3 | Allele length | Assembly | Allele length | hg38 | 370966 | hg19 | 370966 | hg18 | 370966 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv452698, nssv452687, nssv452809, nssv452842, nssv452675 | Samples | NA18916, NA19108, NA19147, HGDP01094, NA19096 | Known Genes | CFH, CFHR1, CFHR2, CFHR3, CFHR4, CFHR5 | 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) | nsv428290
| Frequency | Sample Size | 62 | Observed Gain | 1 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
|
|