Variant DetailsVariant: dgv2776n100Internal ID | 20154392 | Landmark | | Location Information | | Cytoband | 16p12.3 | Allele length | Assembly | Allele length | hg38 | 503946 | hg19 | 503946 | hg18 | 503946 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1036919, nsv1048626, nsv1050063, nsv1035149, nsv1047549, nsv1035531, nsv1039247, nsv1044473 | Samples | | Known Genes | ABCC6, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO3, NPIPA7, NPIPA8, PKD1P1 | 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) | dgv2776n100
| Frequency | Sample Size | 29084 | Observed Gain | 13 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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