Variant DetailsVariant: nsv574700Internal ID | 16015423 | Landmark | | Location Information | | Cytoband | 17q11.2 | Allele length | Assembly | Allele length | hg38 | 1156 | hg19 | 1156 | hg18 | 1156 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv5525n54 | Supporting Variants | nssv869611, nssv869614, nssv869612, nssv869615, nssv869613 | Samples | | Known Genes | CDK5R1 | 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) | nsv574700
| Frequency | Sample Size | 17421 | Observed Gain | 4 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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