Variant DetailsVariant: nsv607736Internal ID | 16048459 | Landmark | | Location Information | | Cytoband | 7q21.12 | Allele length | Assembly | Allele length | hg38 | 3422 | hg19 | 3422 | hg18 | 3422 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv11491n54 | Supporting Variants | nssv1089412, nssv1089411, nssv1089406, nssv1089414, nssv1089426, nssv1089407, nssv1089410, nssv1089404, nssv1089413, nssv1089425, nssv1089408, nssv1089428, nssv1089421, nssv1089422, nssv1089420, nssv1089424, nssv1089418, nssv1089416, nssv1089409, nssv1089423, nssv1089405, nssv1089417, nssv1089427, nssv1089415, nssv1089419 | Samples | | Known Genes | ADAM22 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv607736
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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