Variant DetailsVariant: nssv694658Internal ID | 15084624 | Landmark | | Location Information | | Cytoband | 1q21.3 | Allele length | Assembly | Allele length | hg38 | 447537 | hg19 | 447537 | hg18 | 447537 | hg17 | 447537 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv521887 | Supporting Variants | | Samples | | Known Genes | ADAR, AQP10, ATP8B2, CHRNB2, HAX1, IL6R, KCNN3, SHE, TDRD10, UBAP2L, UBE2Q1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv694658
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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