Variant DetailsVariant: nsv519792Internal ID | 15100399 | Landmark | | Location Information | | Cytoband | Xq21.32 | Allele length | Assembly | Allele length | hg38 | 631416 | hg19 | 631416 | hg18 | 631416 | hg17 | 631416 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv658666, nssv690300, nssv696689, nssv697129, nssv685411, nssv673464, nssv706003, nssv661264 | Samples | | Known Genes | | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv519792
| Frequency | Sample Size | 2026 | Observed Gain | 6 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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