Variant DetailsVariant: nsv1060143Internal ID | 18802674 | Landmark | | Location Information | | Cytoband | 16q22.1 | Allele length | Assembly | Allele length | hg38 | 89759 | hg19 | 89759 | hg18 | 89759 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3001n100 | Supporting Variants | nssv3559494, nssv3559497, nssv3559491, nssv3722738, nssv3559496, nssv3559492, nssv3722737, nssv3722739, nssv3559495, nssv3559493 | Samples | | Known Genes | MIR1972-1, MIR1972-2, PDXDC2P | 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) | nsv1060143
| Frequency | Sample Size | 29084 | Observed Gain | 1 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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