Variant DetailsVariant: nsv515822Internal ID | 15096429 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 14562 | hg19 | 14562 | hg18 | 14562 | hg17 | 14562 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv685701, nssv655746, nssv683659, nssv662338, nssv686967, nssv689011, nssv671249, nssv674886, nssv692342, nssv690087, nssv657332, nssv661213, nssv664886, nssv680579, nssv686541, nssv680026, nssv682010, nssv692138 | Samples | | Known Genes | FAM225B | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515822
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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