Variant DetailsVariant: dgv743n100Internal ID | 20152359 | Landmark | | Location Information | | Cytoband | 10q11.21 | Allele length | Assembly | Allele length | hg38 | 467126 | hg19 | 464415 | hg18 | 464415 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1035291, nsv1051267, nsv1052440, nsv1045328, nsv1045185, nsv1041036, nsv1039765, nsv1045770, nsv1044415, nsv1050198, nsv1046669, nsv1040108, nsv1044607, nsv1055017, nsv1050384, nsv1055118 | Samples | | Known Genes | BMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, 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) | dgv743n100
| Frequency | Sample Size | 29084 | Observed Gain | 24 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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