Pedigree of family UM10qDel-01 and mapping of the 10q deletion by G-banding and FISH. A, Pedigree structure. The arrow identifies the autistic proband. Blackened symbols indicate individuals with the deletion at 10q22.3-q23.31. The dotted line indicates a family member who has not been evaluated. Triangles indicate spontaneous miscarriage. III:3 died of presumed sudden infant death syndrome and was found to have a cardiac defect. B, G-banding and FISH. The left and middle panels show G-banded partial karyotype from one affected individual. The arrow points to the deleted band (10q23.31) (“n” denotes normal chromosome 10; “del” denotes the deletion-bearing chromosome). In the right panel is an example of FISH results from a BAC probe (RP11-926D9) mapping to the breakpoint region that shows a complex pattern of hybridization to the normal and deletion-bearing chromosomes. The normal chromosome 10 shows two closely spaced signals from 10q and an additional signal in a region near the centromere. In the deleted chromosome, the 10q signal is reduced to a single region, and the centromere-associated signal remains. C, Summary of FISH analysis. Chromosome 10 is represented, with a magnification of the region of interest surrounding 10q22.3-q23.31. In the bar representing the deletion map, LCR-containing regions are shown as green boxes, and the deleted sequences are in red. BACs (listed below the map) that did not hybridize to the affected chromosome are in red, BACs that gave the same signal from normal and deleted chromosomes are in black, and BACs from the breakpoint regions that gave multiple signals from normal chromosomes and altered signals from the affected chromosome 10 are in green. The mouse syntenic regions are also represented, with the arrows denoting the orientation of the mouse gene order. Note that breaks in the synteny correspond with the LCR positions.

Whole-genome mapping of deletions in family UM10qDel-01 by use of 100K SNP array and 32K BAC array CGH analyses. A, 100K SNP array analysis. The panel represents SNP copy-number estimates for individual II:1 (fig. 1A). SNP copy number is derived from comparison of SNP intensities for the affected individual with those for unaffected controls by use of the chromosome copy-number tool (Affymetrix). B, 32K BAC array CGH analysis. Log₂ intensity ratios for the same individual (II:1) show the correspondence of the copy-number measures obtained with this methodology. An idiogram of chromosome 10 is represented below the array data.

Breakpoints and models for the rearrangement in JHU10qDel-02. A, Two deletions with an inversion and a small insertion. Diagrams of normal (top) and rearranged (bottom) chromosome 10 are represented. Breakpoint locations for the two identified deletions are indicated by arrows, with nucleotide positions (if known) shown above the arrows. The size of the deletions is indicated between the breakpoints. Beige boxes represent transcripts, brown boxes represent exons, and green boxes represent LCRs. A black dashed line symbolizes a deleted genomic region. This model suggests that sequence flanked by the two deletions is inverted, and fragment 3 (inverted relative to its original orientation) is inserted between the telomeric end of the large deletion and the inversion. Gray block arrows labeled with letters a, b, and c denote sequenced junctions. Sequences containing breakpoints are provided at the bottom of the figure; bold letters indicate junction sequence. B, Two deletions, with three noncontiguous fragments inserted between the end points of the larger one. Diagrams of normal (top) and rearranged (bottom) chromosome 10 are represented. Three fragments (blue block arrow labeled “1,” yellow block arrow labeled “2,” and purple triangle labeled “3”) are inserted between the end points of the large deletion. Size and chromosomal coordinates of the three fragments (1–3) are shown in the key box below. The question mark (?) indicates that the junction sequence is not defined. All other designations are the same as in panel A.

Organization and intrachromosomal distribution of LCRs on 10q22.3-q23.31, along with a map of identified deletions. A, LCRs are grouped into four clusters (LCR1–LCR4). LCR3 and LCR4 flank the 10q22.3-q23.31 deletion in the UM10qDel-01 pedigree and in JHU10qDel-01. Blocks with the same color and/or pattern denote homologous sequences. The degree of sequence identity reflects evolutionary distance and ranges from 90.8% to 99.8%. Genomic position (in Mb) is shown on a scale below the LCRs. Exact chromosome position of depicted LCRs is available from the authors upon request. B, Map of deletions predicted by oligonucleotide array CGH. Three deletions are shown: that in JHU10qDel-01, that in JHU10qDel-02, and a consensus deletion for the two related individuals II:7 and III:6 (from family UM10qDel-01). The gray bar indicates intact DNA sequence. Hemizygous deletions are represented by red dashed lines. The gray dashed lines indicate genomic area that contains the telomeric breakpoints for JHU10qDel-01 and family UM10qDel-01. Genes residing in this genomic region are shown below the deletion map. Full names of the genes shown are given in table 1.

Deletions mapped by oligonucleotide array CGH in four patients: UM10qDel-01 family members III:6 and II:7, JHU10qDel-01 (J1), and JHU10qDel-02 (J2). Oligonucleotide probes (vertical colored bars) are arrayed in horizontal strips for each sample analyzed. In addition to the four patients, array data from three control subjects (C1–C3) are shown. Five different genomic areas (A–E) are arranged in accordance with their position on chromosome 10. LCRs, if present, are depicted as colored boxes below the corresponding probes. Size of the LCRs is proportional to the number of probes present and not to the actual genomic length. Log₂ intensity ratios for each probe are represented in different colors and correspond to the degree of difference between experimental and reference signals. Green, blue, and aqua represent probes with negative log₂ intensity ratios (copy loss), and tan, pink, and red represent probes with positive log₂ intensity ratios (copy gain) in the test sample versus the reference. Red arrows indicate plausible breakpoints of predicted deletions, with genomic position noted above or below the arrows. Panel A shows the region containing the centromeric deletion breakpoint predicted in JHU10qDel-01 (J1), III:6, and II:7. Panel B shows a 96-kb hemizygous deletion predicted in JHU10qDel-02 (J2), which is centromeric to the cytogenetically identified deletion in this patient. Red block arrows indicate sequences that are associated with the end points of the telomeric deletion in JHU10qDel-02. Panel C shows the centromeric deletion breakpoint in JHU10qDel-02 (J2). Panel D contains the telomeric deletion breakpoints for JHU10qDel-01 (J1), III:6, and II:7. Panel E harbors the distal breakpoint for JHU10qDel-02 (J2).