Variant DetailsVariant: dgv740n100Internal ID | 20152356 | Landmark | | Location Information | | Cytoband | 10q11.21 | Allele length | Assembly | Allele length | hg38 | 554823 | hg19 | 552092 | hg18 | 552092 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1037395, nsv1036520, nsv1052860, nsv1047029, nsv1046798, nsv1048332, nsv1041893, nsv1045049, nsv1048338 | Samples | | Known Genes | BMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, PTPN20A, PTPN20B, 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) | dgv740n100
| Frequency | Sample Size | 29084 | Observed Gain | 32 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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