Variant DetailsVariant: nsv971755Internal ID | 18260286 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 1786 | hg19 | 1788 | hg18 | 1788 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2614927, nssv2614933, nssv2614928, nssv2614932, nssv2614924, nssv2614925, nssv2614926, nssv2614931, nssv2614930, nssv2614929 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | BMS1P1, BMS1P5 | Method | Sequencing | Analysis | lineage specific fixed expansions | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv971755
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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