Variant DetailsVariant: nsv515899Internal ID | 15096506 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 234822 | hg19 | 234822 | hg18 | 234822 | hg17 | 234822 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv693083, nssv679688, nssv690694, nssv692622, nssv692354, nssv656683, nssv696532, nssv655701, nssv674489, nssv665191, nssv662159, nssv692817 | Samples | | Known Genes | INIP, KIAA1958, SNX30 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515899
| Frequency | Sample Size | 2026 | Observed Gain | 11 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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