Variant DetailsVariant: nsv972461Internal ID | 18260991 | Landmark | | Location Information | | Cytoband | 9q34.2 | Allele length | Assembly | Allele length | hg38 | 2497 | hg19 | 2497 | hg18 | 2497 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2569621, nssv2569628, nssv2569622, nssv2569624, nssv2569626, nssv2569620, nssv2569625, nssv2569623, nssv2569619, nssv2569627 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | RPL7A, SNORD24, SNORD36A, SNORD36B, SNORD36C | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv972461
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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