Variant DetailsVariant: nsv946951Internal ID | 18247115 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 595 | hg19 | 595 | hg18 | 595 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2598985, nssv2598950, nssv2598982, nssv2598984, nssv2598951, nssv2598946, nssv2598952, nssv2598986, nssv2598945, nssv2598979, nssv2598980, nssv2598981, nssv2598983, nssv2598978, nssv2598953, nssv2598947, nssv2598987, nssv2598954, nssv2598949, nssv2598948 | 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) | nsv946951
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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