Variant DetailsVariant: nsv947996Internal ID | 18248156 | Landmark | | Location Information | | Cytoband | 10q11.23 | Allele length | Assembly | Allele length | hg38 | 7597 | hg19 | 7597 | hg18 | 7597 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1847991, nssv1847998, nssv1847990, nssv1847996, nssv1847993, nssv1847997, nssv1847999, nssv1847995, nssv1847992, nssv1847994 | Samples | HGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665 | Known Genes | | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv947996
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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