Variant DetailsVariant: nssv901807Internal ID | 15849077 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 74568 | hg19 | 74568 | hg18 | 74568 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv580341 | Supporting Variants | | Samples | | Known Genes | GP6, NLRP2, RDH13 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nssv901807
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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