Variant DetailsVariant: dgv5917n100Internal ID | 20157533 | Landmark | | Location Information | | Cytoband | 6p24.2 | Allele length | Assembly | Allele length | hg38 | 69481 | hg19 | 69481 | hg18 | 69481 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1028517, nsv1020564, nsv1029884, nsv1023163, nsv1025443, nsv1018041, nsv1018322, nsv1018741 | Samples | | Known Genes | GCNT2 | 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) | dgv5917n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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