Variant DetailsVariant: nsv946938Internal ID | 18247102 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 749 | hg19 | 749 | hg18 | 749 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2597285, nssv2597289, nssv2597323, nssv2597321, nssv2597316, nssv2597283, nssv2597287, nssv2597324, nssv2597317, nssv2597290, nssv2597320, nssv2597319, nssv2597282, nssv2597322, nssv2597286, nssv2597288, nssv2597281, nssv2597318, nssv2597284, nssv2597315 | 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) | nsv946938
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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