Variant DetailsVariant: nssv1152384Internal ID | 15509387 | Landmark | | Location Information | | Cytoband | 20q11.21 | Allele length | Assembly | Allele length | hg38 | 76801 | hg19 | 76801 | hg18 | 76801 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv585926 | Supporting Variants | | Samples | 1798860570_A | Known Genes | BPIFA2, BPIFA3, BPIFA4P | 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) | nssv1152384
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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