Variant DetailsVariant: nsv946882Internal ID | 18247046 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 754 | hg19 | 754 | hg18 | 754 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2594907, nssv2594940, nssv2594941, nssv2594914, nssv2594908, nssv2594913, nssv2594947, nssv2594943, nssv2594910, nssv2594915, nssv2594939, nssv2594912, nssv2594909, nssv2594942, nssv2594906, nssv2594944, nssv2594911, nssv2594946, nssv2594948, nssv2594945 | 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) | nsv946882
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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