SNP array for CNV calling AUTS2 project [Illumina]. Homo sapiens

Phenotypic and genotypic description of AUTS2 deletion patients found by Array analysis in an international cohort of intellectual disability (ID) and multiple congenital malformations (MCA). Overall design: Arrays were hybridized and analysed using manufacturer's protocols on DNA from patients with ID/MCA本数据集包含在智力障碍（intellectual disability, ID）与多发性先天畸形（multiple congenital malformations, MCA）国际队列中，通过阵列分析（Array analysis）发现的AUTS2缺失患者的表型与基因型特征。实验设计：研究人员依照厂商提供的实验方案，对ID/MCA患者的DNA样本进行阵列杂交与数据分析。