Variant DetailsVariant: nsv946905Internal ID | 18247069 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 596 | hg19 | 658 | hg18 | 658 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2595900, nssv2595960, nssv2595903, nssv2595955, nssv2595956, nssv2595957, nssv2595902, nssv2595963, nssv2595901, nssv2595898, nssv2595897, nssv2595958, nssv2595959, nssv2595899, nssv2595896, nssv2595962, nssv2595905, nssv2595961, nssv2595904, nssv2595954 | 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) | nsv946905
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|