Variant DetailsVariant: nsv523952Internal ID | 15104559 | Landmark | | Location Information | | Cytoband | 11p11.2 | Allele length | Assembly | Allele length | hg38 | 44897 | hg19 | 44897 | hg18 | 44897 | hg17 | 44897 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv699800 | Samples | | Known Genes | PHF21A | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv523952
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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