Variant DetailsVariant: nsv975798Internal ID | 18264319 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 22914 | hg19 | 22914 | hg18 | 22914 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2764830, nssv2759961, nssv2756724, nssv2759811, nssv2762525, nssv2758140, nssv2764667, nssv2759741, nssv2761467 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP00456, HGDP00927 | Known Genes | ANTXRLP1 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv975798
| Frequency | Sample Size | 10 | Observed Gain | 9 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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