Variant DetailsVariant: nssv676200Internal ID | 15066166 | Landmark | | Location Information | | Cytoband | 22q11.21 | Allele length | Assembly | Allele length | hg38 | 2392 | hg19 | 2392 | hg18 | 2392 | hg17 | 2392 |
| Variant Type | CNV loss | Copy Number | | Allele State | Homozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv516997 | Supporting Variants | | Samples | | Known Genes | | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv676200
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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