Variant DetailsVariant: nsv963007Internal ID | 18251563 | Landmark | | Location Information | | Cytoband | 19p13.2 | Allele length | Assembly | Allele length | hg38 | 622 | hg19 | 622 | hg18 | 622 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2133895, nssv2133892, nssv2133893, nssv2133898, nssv2133889, nssv2133891, nssv2133894, nssv2133897, nssv2133896, nssv2133890 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | LOC100289333 | Method | Sequencing | Analysis | lineage specific fixed duplications | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv963007
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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