Variant DetailsVariant: nsv946887Internal ID | 18247051 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 655 | hg19 | 675 | hg18 | 675 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2594226, nssv2594281, nssv2594280, nssv2594288, nssv2594287, nssv2594286, nssv2594229, nssv2594228, nssv2594285, nssv2594282, nssv2594231, nssv2594224, nssv2594225, nssv2594284, nssv2594283, nssv2594223, nssv2594289, nssv2594230, nssv2594222, nssv2594227 | 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) | nsv946887
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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