Variant DetailsVariant: esv2743629Internal ID | 9977913 | Landmark | | Location Information | | Cytoband | 10q26.3 | Allele length | Assembly | Allele length | hg38 | 960 | hg19 | 960 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv115e201 | Supporting Variants | essv6958893, essv6771852, essv6915932, essv6944678, essv6779241, essv6681383, essv6935894, essv6842233 | Samples | SSM065, SSM023, SSM084, SSM021, SSM026, SSM067, SSM033, SSM016 | Known Genes | DPYSL4 | 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) | esv2743629
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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