Internal ID | 20134385 |
Landmark | |
Location Information | |
Cytoband | 10p13 |
Allele length | Assembly | Allele length | hg38 | 117824 | hg19 | 117824 | hg18 | 117824 |
|
Variant Type | CNV gain |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nsv550001, nsv550000, nsv549999 |
Samples | 1782681109_A, 1780862043_A |
Known Genes | DCLRE1C, MEIG1 |
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) | dgv961n54
|
Frequency | Sample Size | 17421 | Observed Gain | 5 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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