Variant DetailsVariant: nsv946886Internal ID | 18247050 | Landmark | | Location Information | | Cytoband | 1q21.1 | Allele length | Assembly | Allele length | hg38 | 710 | hg19 | 710 | hg18 | 710 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2594136, nssv2594133, nssv2594191, nssv2594197, nssv2594196, nssv2594132, nssv2594189, nssv2594194, nssv2594198, nssv2594131, nssv2594135, nssv2594192, nssv2594195, nssv2594139, nssv2594134, nssv2594140, nssv2594193, nssv2594138, nssv2594137, nssv2594190 | 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) | nsv946886
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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