Internal ID | 15527275 |
Landmark | |
Location Information | |
Cytoband | 9q34.11 |
Allele length | Assembly | Allele length | hg38 | 70403 | hg19 | 70403 | hg18 | 70403 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv615412 |
Supporting Variants | |
Samples | HGDP00451 |
Known Genes | C9orf114, ENDOG, TBC1D13, ZER1 |
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) | nssv1176005
|
Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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