Variant DetailsVariant: nsv946883Internal ID | 18247047 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 501 | hg19 | 501 | hg18 | 501 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2595000, nssv2595006, nssv2592941, nssv2592946, nssv2592944, nssv2594999, nssv2594998, nssv2595003, nssv2592945, nssv2594997, nssv2592943, nssv2592942, nssv2592950, nssv2595004, nssv2592948, nssv2592949, nssv2595005, nssv2592947, nssv2595001, nssv2595002 | 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) | nsv946883
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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