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Fig. 1 | Molecular Cytogenetics

Fig. 1

From: Identification of a novel isolated 4q35.2 microdeletion in a Chinese pediatric patient using chromosomal microarray analysis: a case report and literature review

Fig. 1

SNP array detection results in the patient of our study. A The SNP array analysis result demonstrates a 2.0 Mb deletion in 4q35.2 region (arr[GRCh37]4q35.2(188,952,176–190,957,473) × 1), the arrow indicates the deletion region. B In the deletion region, four protein code genes were covered, including TRIML1, TRIML2, FRG1 and FRG2

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