Variant DetailsVariant: dgv7695n100Internal ID | 20159311 | Landmark | | Location Information | | Cytoband | 9q31.1 | Allele length | Assembly | Allele length | hg38 | 47609 | hg19 | 47609 | hg18 | 47609 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1047242, nsv1051839, nsv1047060, nsv1051220, nsv1035258, nsv1039801, nsv1052813 | Samples | | Known Genes | MIR6130 | 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) | dgv7695n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 15 | Observed Complex | 0 | Frequency | n/a |
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