Variant DetailsVariant: dgv812n100Internal ID | 20152428 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 94014 | hg19 | 95140 | hg18 | 95140 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1038700, nsv1053331, nsv1048658, nsv1037371, nsv1052534, nsv1037347, nsv1054931, nsv1038077, nsv1048712, nsv1036538, nsv1045031, nsv1052680, nsv1054598, nsv1047286, nsv1044274 | Samples | | Known Genes | HNRNPA1P33, LINC00842, LOC100996758, NPY4R | 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) | dgv812n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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