Variant DetailsVariant: dgv764n100Internal ID | 20152380 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 210398 | hg19 | 210543 | hg18 | 210543 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1045574, nsv1055122, nsv1054689, nsv1047743, nsv1038133, nsv1038574, nsv1051992, nsv1041317, nsv1044209, nsv1049592 | Samples | | Known Genes | GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15 | 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) | dgv764n100
| Frequency | Sample Size | 29084 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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