Variant DetailsVariant: nssv674095Internal ID | 15064061 | Landmark | | Location Information | | Cytoband | 20q13.12 | Allele length | Assembly | Allele length | hg38 | 111351 | hg19 | 111351 | hg18 | 111351 | hg17 | 111351 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv517296 | Supporting Variants | | Samples | | Known Genes | ACOT8, CTSA, NEURL2, PCIF1, PLTP, SPATA25, ZNF335, ZSWIM1, ZSWIM3 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv674095
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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