Variant DetailsVariant: nsv516198Internal ID | 15096805 | Landmark | | Location Information | | Cytoband | 10p13 | Allele length | Assembly | Allele length | hg38 | 10526 | hg19 | 10526 | hg18 | 10526 | hg17 | 10526 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv672959, nssv677256, nssv683270, nssv681400, nssv693991, nssv662647, nssv662676, nssv668696, nssv655165, nssv661648, nssv657911, nssv662373, nssv692047, nssv700716, nssv690251, nssv659680, nssv666741, nssv687541, nssv681497, nssv683490, nssv661705, nssv659364, nssv668378, nssv656194, nssv672127, nssv684063 | Samples | | Known Genes | CCDC3 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv516198
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 26 | Observed Complex | 0 | Frequency | n/a |
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