Variant DetailsVariant: nsv517631Internal ID | 15098238 | Landmark | | Location Information | | Cytoband | 15q15.1 | Allele length | Assembly | Allele length | hg38 | 90567 | hg19 | 90567 | hg18 | 90567 | hg17 | 90567 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv652598, nssv682320, nssv672157, nssv677235, nssv679020, nssv690496, nssv686868, nssv659851 | Samples | | Known Genes | JMJD7, JMJD7-PLA2G4B, MAPKBP1, MIR4310, PLA2G4B, SPTBN5 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517631
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
|
|