Internal ID | 9904606 |
Landmark | |
Location Information | |
Cytoband | 21q22.3 |
Allele length | Assembly | Allele length | hg38 | 118 | hg19 | 118 |
|
Variant Type | CNV deletion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | esv2723643, esv2723638, esv2723642 |
Supporting Variants | |
Samples | SSM086 |
Known Genes | C21orf2 |
Method | Sequencing |
Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads |
Platform | Illumina HiSeq 2000 |
Comments | |
Reference | Wong_et_al_2012b |
Pubmed ID | 23290073 |
Accession Number(s) | essv6853123
|
Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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