Variant DetailsVariant: esv2733348 | Internal ID | 10316984 | | Landmark | | | Location Information | | | Cytoband | 6q27 | | Allele length | | Assembly | Allele length | | hg38 | 1261 | | hg19 | 1261 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv1040e201 | | Supporting Variants | essv6875861, essv6918994, essv6711983, essv6889277, essv6930605, essv6896874, essv6926945, essv6969532, essv6704776, essv6890339, essv6694329, essv6808552, essv6911491, essv6837582, essv6911490, essv6770970, essv6731022, essv6679966, essv6962640, essv6887132, essv6762265, essv6687384, essv6727266, essv6856331, essv6975055, essv6947960, essv6690611, essv6943603, essv6861041, essv6872892, essv6805563, essv6952056, essv6830319, essv6900376, essv6884351, essv6794812, essv6865770, essv6705168, essv6723380, essv6915198, essv6827209, essv6811436, essv6719583, essv6676726, essv6782364, essv6767656, essv6822581, essv6849360, essv6963975, essv6786546, essv6833914, essv6814464, essv6893662, essv6676725, essv6878726, essv6869895 | | Samples | SSM036, SSM008, SSM083, SSM071, SSM027, SSM024, SSM075, SSM045, SSM046, SSM011, SSM064, SSM079, SSM065, SSM097, SSM093, SSM074, SSM042, SSM088, SSM002, SSM023, SSM028, SSM092, SSM090, SSM047, SSM069, SSM029, SSM096, SSM089, SSM017, SSM019, SSM035, SSM032, SSM044, SSM086, SSM006, SSM068, SSM081, SSM040, SSM082, SSM020, SSM015, SSM016, SSM005, SSM037, SSM077, SSM076, SSM010, SSM091, SSM095, SSM025, SSM004, SSM099, SSM098, SSM012 | | Known Genes | DACT2 | | 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) | esv2733348
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 54 | | Observed Complex | 0 | | Frequency | n/a |
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