Variant DetailsVariant: nssv698196Internal ID | 15088162 | Landmark | | Location Information | | Cytoband | 11q25 | Allele length | Assembly | Allele length | hg38 | 646155 | hg19 | 646154 | hg18 | 646154 | hg17 | 646154 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv521581 | Supporting Variants | | Samples | | Known Genes | ACAD8, B3GAT1, GLB1L2, GLB1L3, JAM3, LOC283177, NCAPD3, THYN1, VPS26B | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv698196
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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