Variant DetailsVariant: nsv517664Internal ID | 15098271 | Landmark | | Location Information | | Cytoband | 11q21 | Allele length | Assembly | Allele length | hg38 | 46890 | hg19 | 46890 | hg18 | 46890 | hg17 | 46890 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv676732, nssv680736, nssv689662, nssv660324, nssv690793, nssv671466, nssv700440, nssv693488, nssv664725, nssv673392, nssv652761, nssv655683, nssv690033, nssv689570 | Samples | | Known Genes | PANX1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517664
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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