Variant DetailsVariant: nsv516338Internal ID | 15096945 | Landmark | | Location Information | | Cytoband | 2p22.3 | Allele length | Assembly | Allele length | hg38 | 21776 | hg19 | 21776 | hg18 | 21776 | hg17 | 21776 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv686069, nssv687561, nssv687715, nssv673029, nssv683321, nssv663151, nssv667684, nssv681597, nssv662625, nssv669532, nssv672626, nssv681284, nssv668701, nssv661187, nssv682327, nssv670556, nssv656030, nssv692651, nssv668355, nssv660562, nssv671643 | Samples | | Known Genes | RASGRP3 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516338
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 21 | Observed Complex | 0 | Frequency | n/a |
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