Variant DetailsVariant: nsv428455 Internal ID | 18278219 | Landmark | | Location Information | | Cytoband | 4q32.3 | Allele length | Assembly | Allele length | hg38 | 402635 | hg19 | 402635 | hg18 | 402635 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv450204, nssv450191, nssv450189, nssv450183, nssv450208, nssv450180, nssv450206, nssv450178, nssv450188, nssv450197, nssv450195, nssv450182, nssv450202, nssv450192, nssv450194, nssv450186, nssv450179, nssv450207, nssv450196, nssv450201, nssv450199, nssv450184, nssv450193, nssv450205, nssv450181, nssv450185, nssv450210, nssv450190, nssv450203, nssv450200 | Samples | HGDP01087, HGDP00462, HGDP01093, HGDP00463, HGDP01088, HGDP01089, NA18916, NA18498, HGDP00476, NA19189, HGDP00460, HGDP00450, HGDP00473, HGDP00986, HGDP00467, NA19181, NA19113, NA19257, NA19225, NA19108, NA19147, HGDP01094, HGDP00984, HGDP00472, HGDP00474, HGDP00471, NA19096, HGDP00478, HGDP01086, HGDP00449 | Known Genes | ANXA10 | 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) | nsv428455
| Frequency | Sample Size | 62 | Observed Gain | 30 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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