Variant DetailsVariant: nsv966272Internal ID | 18254816 | Landmark | | Location Information | | Cytoband | 4q13.1 | Allele length | Assembly | Allele length | hg38 | 11156 | hg19 | 11156 | hg18 | 11156 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2319497, nssv2319494, nssv2319499, nssv2319498, nssv2319492, nssv2319495, nssv2319493, nssv2319491, nssv2319490, nssv2319496 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv966272
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|