Variant DetailsVariant: nsv946921Internal ID | 18247085 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 909 | hg19 | 923 | hg18 | 923 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2595466, nssv2597384, nssv2597387, nssv2595459, nssv2597382, nssv2595464, nssv2595467, nssv2595461, nssv2597389, nssv2597381, nssv2597388, nssv2597380, nssv2595460, nssv2597383, nssv2595462, nssv2595463, nssv2597386, nssv2597385, nssv2595468, nssv2595465 | 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) | nsv946921
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|