Palavra-chave: COPY NUMBER VARIATIONS

8P23.1 DELETION SYNDROME LÚPUS ERITEMATOSO SISTÊMICO 22Q11.2 DISTAL DUPLICATION CONGENITAL HEART DISEASE, HIBRIDAÇÃO GENÔMICA EM ARRAYS 22Q11.2 DELETION SYNDROME CNVS NEUROBEHAVIORAL DISORDERS CHROMOSOMAL MICROARRAY ANALYSIS CNV CYTOGENETICS SÍNDROME VELOCARDIOFACIAL DEFEITOS CARDÍACOS CONGÊNITOS VUS GENOTYPE-PHENOTYPE CORRELATION 22Q11.2 DELETION STRUCTURAL VARIANTS LOW-PASS WHOLE GENOME NEXT GENERATION SEQUENCING (NGS)