Variant DetailsVariant: nsv946884Internal ID | 18247048 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 1281 | hg19 | 1289 | hg18 | 1289 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2593030, nssv2593028, nssv2593089, nssv2593024, nssv2593088, nssv2593083, nssv2593086, nssv2593090, nssv2593022, nssv2593031, nssv2593084, nssv2593029, nssv2593081, nssv2593082, nssv2593025, nssv2593026, nssv2593085, nssv2593027, nssv2593087, nssv2593023 | 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) | nsv946884
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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