Variant DetailsVariant: dgv4448n100Internal ID | 20156064 | Landmark | | Location Information | | Cytoband | 21q22.3 | Allele length | Assembly | Allele length | hg38 | 56792 | hg19 | 56792 | hg18 | 56792 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1066811, nsv1056619, nsv1063344, nsv1061137, nsv1067540 | Samples | | Known Genes | PRMT2 | 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) | dgv4448n100
| Frequency | Sample Size | 29084 | Observed Gain | 7 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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