Internal ID | 16047521 |
Landmark | |
Location Information | |
Cytoband | 7p13 |
Allele length | Assembly | Allele length | hg38 | 273 | hg19 | 273 | hg18 | 273 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | dgv11309n54 |
Supporting Variants | nssv1083537, nssv1083539, nssv1083538, nssv1083540 |
Samples | |
Known Genes | CAMK2B |
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) | nsv606798
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
|