Variant DetailsVariant: nsv975697Internal ID | 18264218 | Landmark | | Location Information | | Cytoband | 10q11.23 | Allele length | Assembly | Allele length | hg38 | 6524 | hg19 | 6524 | hg18 | 6524 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2613431, nssv2613430, nssv2613426, nssv2613427, nssv2613424, nssv2613425, nssv2613429, nssv2613428, nssv2613433, nssv2613432 | Samples | HGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927 | Known Genes | AGAP7 | Method | Sequencing | Analysis | lineage specific fixed expansions | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nsv975697
| Frequency | Sample Size | 10 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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