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Correction: Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease
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https://doi.org/10.1136/archdischild-2018-316634corr1

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    Hou H, Chen H, Wang X, et al. Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease. Arch Dis Child 2020;105:367-74.

    During production of this paper, two errors were introduced in the numbers of table 1. The numbers highlighted in red should be 17.3 and 19.2 respectively instead of 1.7 and 1.9.

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    Table 1

    Phenotypic characteristics of all patients with CHD and the percentage of 22q11.2 deletions or amplifications in each group

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