Variant DetailsVariant: essv6985826Internal ID | 12637414 | Landmark | | Location Information | | Cytoband | 7q22.1 | Allele length | Assembly | Allele length | hg38 | 428816 | hg19 | 428816 | hg18 | 428816 | hg17 | 428816 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2752138 | Supporting Variants | | Samples | SPC_61 | Known Genes | ARMC10, FAM185A, FBXL13, LRRC17, NAPEPLD, RPL19P12 | Method | SNP array | Analysis | | Platform | Affymetrix Mapping 250K Nsp SNP Array | Comments | | Reference | Pinto_et_al_2007 | Pubmed ID | 17911159 | Accession Number(s) | essv6985826
| Frequency | Sample Size | 771 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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