Internal ID | 15037813 |
Landmark | |
Location Information | |
Cytoband | 6p24.2 |
Allele length | Assembly | Allele length | hg38 | 50353 | hg19 | 50353 | hg18 | 50353 | hg16 | 50353 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv437958 |
Supporting Variants | |
Samples | NA10863 |
Known Genes | GCNT2 |
Method | SNP array |
Analysis | Mendelian inconsistencies - for each genotype assay and population sample we defined the Mendel failure pattern of that assay as the binary vector (length 60) of Mendel consistency status across the 60 parent-offspring pair. |
Platform | Not reported |
Comments | |
Reference | McCarroll_et_al_2006 |
Pubmed ID | 16468122 |
Accession Number(s) | nssv468717
|
Frequency | Sample Size | 269 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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