Variant DetailsVariant: nsv967821Internal ID | 18256363 | Landmark | | Location Information | | Cytoband | 4p16.3 | Allele length | Assembly | Allele length | hg38 | 43521 | hg19 | 43413 | hg18 | 43413 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2691771, nssv2691770, nssv2691764, nssv2691765, nssv2691762, nssv2691767, nssv2691768, nssv2691769, nssv2691763, nssv2691766 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | ZNF595, ZNF718 | Method | Sequencing | Analysis | lineage specific fixed expansions | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv967821
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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