Variant DetailsVariant: nssv688470Internal ID | 15078436 | Landmark | | Location Information | | Cytoband | 20p13 | Allele length | Assembly | Allele length | hg38 | 87462 | hg19 | 87462 | hg18 | 87462 | hg17 | 87462 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv520565 | Supporting Variants | | Samples | | Known Genes | ADAM33, GFRA4, HSPA12B, SIGLEC1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv688470
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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