Variant DetailsVariant: nsv946922Internal ID | 18247086 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 1138 | hg19 | 1170 | hg18 | 1170 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2597473, nssv2597481, nssv2597418, nssv2597477, nssv2597472, nssv2597417, nssv2597413, nssv2597415, nssv2597480, nssv2597479, nssv2597419, nssv2597476, nssv2597422, nssv2597414, nssv2597421, nssv2597478, nssv2597420, nssv2597474, nssv2597416, nssv2597475 | 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) | nsv946922
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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