Variant DetailsVariant: nsv1064467Internal ID | 18806998 | Landmark | | Location Information | | Cytoband | 19q13.31 | Allele length | Assembly | Allele length | hg38 | 185588 | hg19 | 185588 | hg18 | 185588 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3591n100 | Supporting Variants | nssv3724619, nssv3724622, nssv3574243, nssv3574241, nssv3724614, nssv3724624, nssv3724613, nssv3574238, nssv3724618, nssv3574239, nssv3574234, nssv3574233, nssv3724616, nssv3574242, nssv3574231, nssv3724615, nssv3574240, nssv3724623, nssv3574235, nssv3574230, nssv3574232, nssv3724621, nssv3574237, nssv3724620, nssv3724617, nssv3574236 | Samples | | Known Genes | LOC284344, PSG4, PSG5, PSG9 | 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) | nsv1064467
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 26 | Observed Complex | 0 | Frequency | n/a |
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