Variant DetailsVariant: dgv2502n100Internal ID | 20154118 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 377483 | hg19 | 377483 | hg18 | 377483 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1053426, nsv1053477, nsv1049228, nsv1042887, nsv1051358, nsv1054072, nsv1038913, nsv1047149, nsv1049267, nsv1050200, nsv1038635, nsv1039443, nsv1036631 | Samples | | Known Genes | CHRFAM7A, DKFZP434L187, LOC101059918 | 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) | dgv2502n100
| Frequency | Sample Size | 29084 | Observed Gain | 34 | Observed Loss | 95 | Observed Complex | 0 | Frequency | n/a |
|
|