Variant DetailsVariant: nsv1056795Internal ID | 18799326 | Landmark | | Location Information | | Cytoband | 17p13.1 | Allele length | Assembly | Allele length | hg38 | 87403 | hg19 | 87403 | hg18 | 87403 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3095n100 | Supporting Variants | nssv3560332, nssv3560331, nssv3719161, nssv3560329, nssv3560328, nssv3560330, nssv3719160 | Samples | | Known Genes | ALOX12P2 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | nsv1056795
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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