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Blood, Vol. 111, Issue 3, 1029-1038, February 1, 2008
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura
Blood Breunis et al.
111: 1029
Supplemental materials for: Breunis et al
Files in this Data Supplement:
- Table S1. MLPA probes (PDF, 16.3 KB)
- Figure S1. CNV in FCGR3B (PDF, 21.7 KB) -
MLPA electropherogram. Individual A with only 1 allele FCGR3B (grey line) compared to individual B with 2 alleles of FCGR3B (black line). FCGR3B specific probes are indicated with an arrow. As an example 2 of the control probes are indicated (C). On of the probes is specific for the X-chromosome (X). Individual A (grey): Male, FCGR3B-Na1, FCGR3A-158FF. Individual B (black): Female, FCGR3B-Na1Na2, FCGR3A-158FF.
- Figure S2. CNV in FCGR3B (PDF, 23.9 KB) -
MLPA electropherogram. Individual C with only 3 alleles FCGR3B (grey line) compared to individual B with 2 alleles of FCGR3B (black line). FCGR3B specific probes are indicated with an arrow. As an example 2 of the control probes are indicated (C). One of the probes is specific for the X-chromosome (X). Individual C (grey): Female, FCGR3B-Na1Na2Na2, FCGR3A-158FF. Individual B (black): Female, FCGR3B-Na1Na2, FCGR3A-158FF.
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