SNP data from 13 childhood adrenocortical tumours from Brazilian patients and 6 matched normal samples. Homo sapiens

SNP array data from 13 Brazilian childhood adrenocortical tumors (ACTs) were analyzed to detect recurrent copy number changes and highlight potential candidate driver genes. Overall design: 13 childhood ACT were analyzed with Illumina HumanCNV370-Duo v1.0 chips. Paired normal blood samples from 6 patients were analyzed with Illumina HumanCNV370-Quad v3.0 chips.

本研究对13例巴西儿童肾上腺皮质肿瘤（adrenocortical tumor, ACT）的单核苷酸多态性阵列（SNP array）数据进行分析，旨在检测复发性拷贝数变异，并筛选潜在的候选驱动基因。实验整体设计如下：13例儿童肾上腺皮质肿瘤样本均采用Illumina HumanCNV370-Duo v1.0芯片进行检测；其中6例患者的配对正常血液样本采用Illumina HumanCNV370-Quad v3.0芯片完成检测分析。