Variant DetailsVariant: dgv7466n100Internal ID | 20159082 | Landmark | | Location Information | | Cytoband | 9p22.2 | Allele length | Assembly | Allele length | hg38 | 59534 | hg19 | 59534 | hg18 | 59534 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1022691, nsv1032604, nsv1030902, nsv1029253, nsv1015810, nsv1017917, nsv1024129, nsv1021448, nsv1031193, nsv1019764, nsv1025072, nsv1033807 | Samples | | Known Genes | SH3GL2 | 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) | dgv7466n100
| Frequency | Sample Size | 29084 | Observed Gain | 29 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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