Variant DetailsVariant: nssv685418Internal ID | 15075384 | Landmark | | Location Information | | Cytoband | 17q25.1 | Allele length | Assembly | Allele length | hg38 | 342491 | hg19 | 342491 | hg18 | 342491 | hg17 | 342491 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv516133 | Supporting Variants | | Samples | | Known Genes | CASKIN2, GALK1, ITGB4, KIAA0195, LLGL2, MIR6785, MYO15B, RECQL5, SAP30BP, SMIM5, SMIM6, TSEN54 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv685418
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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