Variant DetailsVariant: nsv946895Internal ID | 18247059 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 715 | hg19 | 727 | hg18 | 727 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2595509, nssv2595503, nssv2595504, nssv2595542, nssv2595534, nssv2595502, nssv2595501, nssv2595539, nssv2595508, nssv2595510, nssv2595543, nssv2595537, nssv2595505, nssv2595538, nssv2595535, nssv2595536, nssv2595541, nssv2595506, nssv2595540, nssv2595507 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | LOC101929780, NBPF10, NBPF14, NBPF8, NBPF9 | Method | Sequencing | Analysis | lineage specific fixed expansions | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv946895
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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